Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125445771 | 12544577 | 1 | I | 201511 | 20151201 | 20160711 | 20160711 | PER | US-DSJP-DSU-2015-137598 | DAIICHI | 78.64 | YR | F | Y | 58.96000 | KG | 20160711 | MD | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125445771 | 12544577 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/12.5 MG, QD | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
| 125445771 | 12544577 | 2 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 75 ?G, QD | 0 | 75 | UG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125445771 | 12544577 | 1 | Hypertension |
| 125445771 | 12544577 | 2 | Hypothyroidism |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125445771 | 12544577 | Asthenia | |
| 125445771 | 12544577 | Dizziness | |
| 125445771 | 12544577 | Fatigue | |
| 125445771 | 12544577 | Hypotension | |
| 125445771 | 12544577 | Muscle spasms | |
| 125445771 | 12544577 | Myalgia | |
| 125445771 | 12544577 | Nausea | |
| 125445771 | 12544577 | Pain | |
| 125445771 | 12544577 | Somnolence |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |